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Naphthalene-1,4-diylbis(trimethylsilane) is an organosilicon compound with the chemical formula C16H24Si2. It is a white crystalline solid that is insoluble in water but soluble in organic solvents. naphthalene-1,4-diylbis(trimethylsilane) is formed by the attachment of two trimethylsilyl groups to the 1 and 4 positions of a naphthalene molecule. Naphthalene-1,4-diylbis(trimethylsilane) is primarily used as a reagent in organic synthesis, particularly in the preparation of various naphthalene derivatives. It is also employed as a protecting group in the synthesis of complex organic molecules, as the trimethylsilyl groups can be easily removed under mild conditions, allowing for selective functionalization of the naphthalene core. Due to its stability and reactivity, naphthalene-1,4-diylbis(trimethylsilane) has found applications in the pharmaceutical and materials science industries.

1024-47-1

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1024-47-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1024-47-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,2 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1024-47:
(6*1)+(5*0)+(4*2)+(3*4)+(2*4)+(1*7)=41
41 % 10 = 1
So 1024-47-1 is a valid CAS Registry Number.

1024-47-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl-(4-trimethylsilylnaphthalen-1-yl)silane

1.2 Other means of identification

Product number -
Other names Silane,1,4-naphthalenediylbis(trimethyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1024-47-1 SDS

1024-47-1Downstream Products

1024-47-1Relevant academic research and scientific papers

Absorption and fluorescence spectroscopic properties of 1- and 1,4-silyl-substituted naphthalene derivatives

Maeda, Hajime,Maeda, Tomohiro,Mizuno, Kazuhiko

, p. 5108 - 5125 (2012)

Silyl-substituted naphthalene derivatives at the 1- and 1,4-positions were synthesized and their UV absorption, fluorescence spectroscopic properties, and fluorescence lifetimes were determined. Analysis of the results shows that the introduction of silyl groups at these positions of the naphthalene chromophore/fluorophore causes shifts of the absorption maxima to longer wavelengths and increases in fluorescence intensities. Bathochromic shifts of the absorption maxima and increases in fluorescence intensities are also promoted by the introduction of methoxy and cyano groups at the naphthalene 4- and 5-positions. In addition, the fluorescence of 9,10-dicyanoanthracene is efficiently quenched by these naphthalene derivatives with Stern-Volmer plot calculated rate constants that depend on the steric bulk of the silyl groups.

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